Variant report

Variant	nsv879841
Chromosome Location	chr4:120244085-120388406
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1328)
CpG islands
(count:734)
Chromatin interactive
region (count:5)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1328 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:120292324-120292770	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:120375640-120376007	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:120375657-120375939	K562	blood:	n/a	n/a
4	ATF1	chr4:120375410-120376174	K562	blood:	n/a	n/a
5	ATF1	chr4:120324198-120324405	K562	blood:	n/a	n/a
6	ATF2	chr4:120375554-120376118	H1-hESC	embryonic stem cell:	n/a	chr4:120375758-120375769
7	ATF2	chr4:120375508-120376132	GM12878	blood:	n/a	chr4:120375758-120375769
8	ATF2	chr4:120375574-120376077	H1-hESC	embryonic stem cell:	n/a	chr4:120375758-120375769
9	ATF2	chr4:120375555-120376037	GM12878	blood:	n/a	chr4:120375758-120375769
10	ATF2	chr4:120291443-120291898	GM12878	blood:	n/a	n/a
11	ATF3	chr4:120375748-120376028	GM12878	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
12	ATF3	chr4:120375689-120376103	HepG2	liver:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
13	ATF3	chr4:120375570-120376147	H1-hESC	embryonic stem cell:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
14	ATF3	chr4:120375667-120376101	K562	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
15	ATF3	chr4:120375643-120376128	GM12878	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
16	ATF3	chr4:120376142-120376354	K562	blood:	n/a	n/a
17	ATF3	chr4:120375591-120376108	K562	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
18	ATF3	chr4:120375697-120376130	H1-hESC	embryonic stem cell:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
19	ATF3	chr4:120375585-120375981	A549	lung:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
20	ATF3	chr4:120375534-120376115	HepG2	liver:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
21	BACH1	chr4:120375824-120376166	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr4:120383409-120383814	GM12878	blood:	n/a	n/a
23	BATF	chr4:120377931-120378220	GM12878	blood:	n/a	n/a
24	BATF	chr4:120383430-120383818	GM12878	blood:	n/a	n/a
25	BATF	chr4:120336031-120336269	GM12878	blood:	n/a	n/a
26	BATF	chr4:120375371-120376260	GM12878	blood:	n/a	n/a
27	BATF	chr4:120377964-120378201	GM12878	blood:	n/a	n/a
28	BATF	chr4:120288050-120288247	GM12878	blood:	n/a	n/a
29	BATF	chr4:120291572-120291901	GM12878	blood:	n/a	n/a
30	BATF	chr4:120295932-120296203	GM12878	blood:	n/a	chr4:120296096-120296107
31	BATF	chr4:120291551-120292008	GM12878	blood:	n/a	n/a
32	BCL11A	chr4:120383416-120384004	GM12878	blood:	n/a	chr4:120383850-120383859
33	BCL11A	chr4:120291635-120291957	GM12878	blood:	n/a	n/a
34	BCL11A	chr4:120375997-120376209	GM12878	blood:	n/a	n/a
35	BCL11A	chr4:120378027-120378298	GM12878	blood:	n/a	n/a
36	BCL11A	chr4:120375469-120376323	GM12878	blood:	n/a	n/a
37	BCL3	chr4:120375586-120376104	A549	lung:	n/a	n/a
38	BCLAF1	chr4:120375555-120376089	GM12878	blood:	n/a	n/a
39	BCLAF1	chr4:120375644-120376123	GM12878	blood:	n/a	n/a
40	BHLHE40	chr4:120292531-120292706	HepG2	liver:	n/a	n/a
41	BHLHE40	chr4:120375666-120376228	K562	blood:	n/a	n/a
42	BHLHE40	chr4:120375682-120376067	GM12878	blood:	n/a	n/a
43	BRCA1	chr4:120375591-120376075	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr4:120375657-120376065	H1-hESC	embryonic stem cell:	n/a	n/a
45	BRCA1	chr4:120375670-120376051	GM12878	blood:	n/a	n/a
46	BRCA1	chr4:120375681-120376092	HepG2	liver:	n/a	n/a
47	CBX3	chr4:120374867-120376298	K562	blood:	n/a	n/a
48	CBX3	chr4:120309985-120310304	K562	blood:	n/a	n/a
49	CBX3	chr4:120375690-120376086	HCT-116	colon:	n/a	n/a
50	CBX3	chr4:120375579-120376037	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120375747-120375797	H1-hESC	embryonic stem cell:	embryo
2	chr4:120376055-120376105	NHBE	bronchial:	n/a
3	chr4:120375747-120375797	H1-hESC	embryonic stem cell:	embryo
4	chr4:120376055-120376105	NHBE	bronchial:	n/a
5	chr4:120332083-120332133	NB4	blood:	n/a
6	chr4:120329925-120329975	MCF-7	breast:	n/a
7	chr4:120378622-120378672	HCT-116	colon:	n/a
8	chr4:120375997-120376047	BE2_C	brain:	n/a
9	chr4:120378622-120378672	HEK293	kidney:	embryo
10	chr4:120328025-120328075	SAEC	small airway:	n/a
11	chr4:120376055-120376105	RPTEC	kidney:	n/a
12	chr4:120332083-120332133	HMEC	breast:	n/a
13	chr4:120332083-120332133	SK-N-SH	brain:	n/a
14	chr4:120329925-120329975	HRE	kidney:	n/a
15	chr4:120375997-120376047	HMEC	breast:	n/a
16	chr4:120373434-120373484	HCPEpiC	choroid plexus:	n/a
17	chr4:120376055-120376105	PrEC	prostate:	n/a
18	chr4:120376055-120376105	PANC-1	pancreas:	n/a
19	chr4:120329925-120329975	PrEC	prostate:	n/a
20	chr4:120375747-120375797	K562	blood:	n/a
21	chr4:120376055-120376105	HMEC	breast:	n/a
22	chr4:120375409-120375459	A549	lung:	n/a
23	chr4:120376271-120376321	CMK	blood:	n/a
24	chr4:120327624-120327674	ovcar-3	ovarian:	n/a
25	chr4:120375747-120375797	HCM	heart:	n/a
26	chr4:120375409-120375459	CMK	blood:	n/a
27	chr4:120375997-120376047	HNPCEpiC	eye:	n/a
28	chr4:120376271-120376321	U87	brain:	n/a
29	chr4:120328025-120328075	SK-N-MC	brain:	n/a
30	chr4:120329925-120329975	Caco-2	colon:	n/a
31	chr4:120332083-120332133	A549	lung:	n/a
32	chr4:120376055-120376105	SK-N-SH_RA	brain:	n/a
33	chr4:120327624-120327674	K562	blood:	n/a
34	chr4:120376271-120376321	NT2-D1	testis:	n/a
35	chr4:120375409-120375459	HEEpiC	esophagus:	n/a
36	chr4:120376271-120376321	ovcar-3	ovarian:	n/a
37	chr4:120376271-120376321	HL-60	blood:	n/a
38	chr4:120328025-120328075	CMK	blood:	n/a
39	chr4:120327182-120327232	CMK	blood:	n/a
40	chr4:120328025-120328075	AG04450	lung:	fetal
41	chr4:120373434-120373484	HRPEpiC	eye:	n/a
42	chr4:120375409-120375459	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:120375747-120375797	HRCEpiC	kidney:	n/a
44	chr4:120376271-120376321	NB4	blood:	n/a
45	chr4:120378622-120378672	HCM	heart:	n/a
46	chr4:120327624-120327674	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:120332083-120332133	HCPEpiC	choroid plexus:	n/a
48	chr4:120375747-120375797	SK-N-MC	brain:	n/a
49	chr4:120327182-120327232	HEK293	kidney:	embryo
50	chr4:120373434-120373484	LNCaP	prostate:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:120249451..120251294-chr4:120987361..120988915,2	K562	blood:
2	chr4:120132920..120134685-chr4:120374052..120375829,2	K562	blood:
3	chr4:120132920..120134685-chr4:120374052..120375829,3	K562	blood:
4	chr4:120372429..120374699-chr4:120400382..120402462,2	K562	blood:
5	chr4:119679216..119681142-chr4:120375525..120377542,2	MCF-7	breast:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC110373.1-2	chr4:120330489-120331408	NONHSAT098058
2	lnc-AC110373.1-8	chr4:120381592-120381982	NONHSAT098080
3	lnc-AC110373.1-8	chr4:120384051-120384134	NONHSAT098082
4	lnc-AC110373.1-8	chr4:120381834-120381982	NONHSAT098082
5	lnc-AC110373.1-8	chr4:120382872-120383006	NONHSAT098081
6	lnc-AC110373.1-3	chr4:120377948-120378432	ENSG00000250950.1
7	lnc-PDE5A-3	chr4:120365524-120365586	NONHSAT098064
8	lnc-PDE5A-3	chr4:120375401-120375783	NONHSAT098065
9	lnc-AC110373.1-8	chr4:120382872-120383006	NONHSAT098079
10	lnc-PDE5A-3	chr4:120362106-120362207	NONHSAT098064
11	lnc-AC110373.1-2	chr4:120330488-120331388	ENSG00000260091.1
12	lnc-PDE5A-3	chr4:120361716-120361790	NONHSAT098064
13	lnc-AC110373.1-3	chr4:120377505-120377592	ENSG00000250950.1
14	lnc-AC110373.1-8	chr4:120384051-120384134	NONHSAT098079
15	lnc-AC110373.1-8	chr4:120381367-120381397	NONHSAT098079
16	lnc-AC110373.1-8	chr4:120382872-120383019	NONHSAT098078
17	lnc-AC110373.1-8	chr4:120381886-120381982	NONHSAT098079
18	lnc-PDE5A-3	chr4:120371197-120371312	NONHSAT098064
19	lnc-AC110373.1-8	chr4:120381898-120381975	NONHSAT098078
20	lnc-AC110373.1-8	chr4:120382872-120383065	NONHSAT098080
21	lnc-AC110373.1-8	chr4:120379123-120379232	NONHSAT098078
22	lnc-AC110373.1-8	chr4:120381811-120381982	NONHSAT098081
23	lnc-PDE5A-3	chr4:120370725-120371280	NONHSAT098065
24	lnc-AC110373.1-8	chr4:120384051-120384134	NONHSAT098081
25	lnc-AC110373.1-8	chr4:120382872-120383006	NONHSAT098082

No data

Variant related genes	Relation type
ENSG00000260091	TF binding region
RNU6-1217P	TF binding region
ENSG00000250950	TF binding region
RNU4-33P	TF binding region
FABP2	TF binding region
ENSG00000248280	TF binding region
ENSG00000249244	TF binding region
ENSG00000245958	TF binding region
KLHL2P1	TF binding region
ENSG00000260091	CpG island
RNU6-1217P	CpG island
ENSG00000250950	CpG island
RNU4-33P	CpG island
FABP2	CpG island
ENSG00000248280	CpG island
ENSG00000249244	CpG island
ENSG00000245958	CpG island
KLHL2P1	CpG island
ENSG00000164109	chromatin interactions
ENSG00000150961	chromatin interactions
ENSG00000250938	chromatin interactions
ENSG00000178636	chromatin interactions
ENSG00000145390	chromatin interactions

Extended variants
information (count: 4911 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4911 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10034661	chr4:120244085-120244086	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574344212	chr4:120244097-120244098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543359078	chr4:120244099-120244100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540886804	chr4:120244125-120244126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13306357	chr4:120244134-120244135	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs576392607	chr4:120244183-120244184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114129584	chr4:120244233-120244234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113133497	chr4:120244237-120244238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565282011	chr4:120244350-120244351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs28441186	chr4:120244438-120244439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184991757	chr4:120244454-120244455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs13101526	chr4:120244456-120244457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
13	rs34605419	chr4:120244464-120244465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200834322	chr4:120244467-120244468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10013042	chr4:120244482-120244483	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs146511169	chr4:120244495-120244496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529121989	chr4:120244497-120244498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375022078	chr4:120244499-120244500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575271678	chr4:120244502-120244503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548897109	chr4:120244532-120244533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs61574855	chr4:120244573-120244574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs199908041	chr4:120244574-120244575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs55884612	chr4:120244577-120244578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs373735748	chr4:120244580-120244581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551456126	chr4:120244581-120244582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376380126	chr4:120244583-120244584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371070337	chr4:120244588-120244589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375114344	chr4:120244591-120244592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368454714	chr4:120244592-120244593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540178512	chr4:120244604-120244605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372310680	chr4:120244605-120244606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190439776	chr4:120244620-120244621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs180882068	chr4:120244626-120244627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186236136	chr4:120244629-120244630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs56166638	chr4:120244648-120244649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571209051	chr4:120244662-120244663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs35917388	chr4:120244663-120244664	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs181297399	chr4:120244685-120244686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543587062	chr4:120244698-120244699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567881780	chr4:120244719-120244720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112016690	chr4:120244724-120244725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs59036484	chr4:120244749-120244750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556936836	chr4:120244781-120244782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2389746	chr4:120244850-120244851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs202156486	chr4:120244856-120244857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs376332368	chr4:120244872-120244873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369906708	chr4:120244886-120244887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141105010	chr4:120244893-120244894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs71627784	chr4:120244902-120244903	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs558918755	chr4:120244930-120244931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120222000-120251000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr4:120222200-120244600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:120235600-120251000	Weak transcription	Left Ventricle	heart
4	chr4:120243400-120244200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr4:120243600-120245200	Enhancers	Fetal Intestine Large	intestine
6	chr4:120243800-120244200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr4:120243800-120244400	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr4:120244000-120244400	Enhancers	Duodenum Mucosa	Duodenum
9	chr4:120244000-120245400	Enhancers	Fetal Intestine Small	intestine
10	chr4:120244400-120244800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr4:120244400-120249800	Weak transcription	Duodenum Mucosa	Duodenum
12	chr4:120244800-120245200	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr4:120245000-120245200	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr4:120245200-120249600	Weak transcription	Fetal Intestine Large	intestine
15	chr4:120245400-120249600	Weak transcription	Fetal Intestine Small	intestine
16	chr4:120248800-120249400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:120249600-120250000	Enhancers	Fetal Intestine Large	intestine
18	chr4:120249600-120250200	Enhancers	Fetal Intestine Small	intestine
19	chr4:120249800-120250000	Enhancers	Duodenum Mucosa	Duodenum
20	chr4:120249800-120252800	Enhancers	Fetal Heart	heart
21	chr4:120250000-120250800	Weak transcription	Duodenum Mucosa	Duodenum
22	chr4:120250000-120251000	Weak transcription	Fetal Intestine Large	intestine
23	chr4:120250200-120250600	Weak transcription	Fetal Intestine Small	intestine
24	chr4:120250600-120251600	Enhancers	Fetal Intestine Small	intestine
25	chr4:120250800-120251800	Enhancers	Duodenum Mucosa	Duodenum
26	chr4:120251000-120251200	Enhancers	Left Ventricle	heart
27	chr4:120251000-120251600	Enhancers	Fetal Intestine Large	intestine
28	chr4:120251000-120251800	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr4:120251200-120257600	Weak transcription	Left Ventricle	heart
30	chr4:120251800-120258000	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr4:120253800-120254000	Enhancers	Esophagus	oesophagus
32	chr4:120254000-120254200	Weak transcription	Esophagus	oesophagus
33	chr4:120256800-120258000	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr4:120256800-120259000	Enhancers	Spleen	Spleen
35	chr4:120257000-120257200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr4:120257000-120258400	Enhancers	HMEC	breast
37	chr4:120257600-120257800	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr4:120257600-120258400	Enhancers	NHEK	skin
39	chr4:120257600-120259000	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr4:120257800-120258400	Weak transcription	Left Ventricle	heart
41	chr4:120257800-120258600	Enhancers	HUVEC	blood vessel
42	chr4:120257800-120258600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr4:120258000-120258200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr4:120258000-120258400	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr4:120258000-120259000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr4:120258200-120258600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr4:120258200-120259000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr4:120258200-120259200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr4:120258600-120259000	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr4:120258800-120259000	Enhancers	Left Ventricle	heart

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